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Portal about the device of the sewerage and drainpipes
  • Centrifugal Pump Performance
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  • Anolyte is neutral. Anolyte neutral anch.

    Anolyte is neutral. Anolyte neutral anch.

    The Aquamed installation is intended for preparation of highly effective, environmentally safe and cost-effective disinfecting and washing solutions. It is a reliable and safe alternative to traditional disinfectants and detergents. "Aquamed" allows you to get rid of the problems of the acquisition, transportation, storage and accounting of disinfectants. At any time you will have as much disinfectant solution as you need!

    The installation was developed in conjunction with the Department of General Hygiene and Ecology of the Voronezh State Medical University and is intended for the electrochemical conversion of water-salt solutions of chlorides into a metastable activated disinfectant solution - neutral anolyte (registry. Certificate No. 08-33-0.232467), which contains the active substances represented by the products of anodic oxidation of water hydrogen and sodium chloride (HClO, HClO2, ClO2, H2 O2, HO2, O3, O2, HO).

    The department, together with the Vitebsk OCHEiOZ, the Republican Scientific and Research Center for Hygiene and the Research Institute of Epidemiology and Microbiology, has established the high bactericidal, tuberculocidal, virucidal and fungicidal activity of the neutral anolyte, which meets the requirements of SanPiN 21-112-99 for safety and efficacy of disinfectants.

    Neutral Anolyte is intended for disinfection in medical and preventive and pharmaceutical institutions, trade enterprises, public catering and market entities, hotels and hostels, as well as for disinfection of swimming pool water in accordance with instructions approved and registered with the Ministry of Health.

    Neutral anolyte, having high biocidal activity, is environmentally friendly at the same time, does not accumulate in the environment, is produced from accessible and cheap components. Safety is given to the anolyte by a low concentration of active substances, and environmental friendliness is its natural property to relax spontaneously without the formation of toxic xenobiotic compounds, and neutralization after use is not required.

    For the operation of the installation, a pressure source of drinking water, table salt and a voltage of ~ 220V are required.

    The use of the Aquamed installation is economically viable. For example, to prepare 200 liters of neutral anolyte, it is necessary to spend 1 kg of sodium chloride and 1 kW of electricity, i.e. the current cost of preparing 1 liter of neutral anolyte is about 1 ruble.

    The neutral anolyte obtained at the Aquamed installation surpasses the similar solution prepared in the domestic production of the BAVR type and the Russian-made installations of the STEL, EHA-30, REDO-MT2 type and others, in terms of performance the effect of disinfecting objects is achieved with a lower concentration of active substances in the solution and with a shorter exposure time. At the same time, the price of the Aquamed installation is lower than the indicated analogues.

    Currently, the installation "Aquamed" successfully used dozens of medical and sanatorium institutions of the country.

    There is all the necessary regulatory documentation for the installation and neutral anolyte.


    INSTRUCTIONS on the use of a neutral anolyte disinfectant solution, obtained on installations like "AQUAMED" in medical and preventive organizations

    INSTRUCTION was developed by Vitebsk State Medical University, Scientific Research Institute of Sanitation and Hygiene, Vitebsk Regional Center for Hygiene, Epidemiology and Public Health, Vitebsk City Center of Hygiene and Epidemiology, Scientific and Production Unitary Enterprise “AQUAPRIBOR”.

    Authors: I.I. Burak, V.I. Klyuchenovich, A.Yurkevich, N.V. Zheleznyak, N.I. Miklis, L.V. Polovinkin, A.S. Ananiev, L.V. Shunko, N. Ya.Krasovsky, N.A. Tatarenko.

    The INSTRUCTION is intended for personnel of health care organizations, disinfection centers, hygiene and epidemiology centers, and other institutions involved in disinfection activities.

    1. General information

    1.1. Neutral anolyte is a transparent liquid with a faint smell of chlorine, the main active components of which are highly active oxygen compounds of chlorine (ClO 2, HclO, NaCIO, HClO 2, NaClO 2, etc.).

    1.2. A neutral anolyte disinfectant solution is obtained by electrochemical activation in Aquamed installations (TU RB 490085159.002.2003) from aqueous solutions of chlorides (NaCl, KC1, etc.) in accordance with the Operation Manual. The installation allows you to get anolyte with an active chlorine content of 200 - 400 mg / DM 3 and pH \u003d 6.2 - 7.2.

    1.3. The quality control of the neutral anolyte is carried out upon commissioning of the installation and subsequently monthly in the chemical laboratory, and self-monitoring is carried out daily and when the operating mode is changed by the express method in accordance with Appendix 1.

    1.4. Prepared solutions of neutral anolyte are stored in sealed containers of inert materials (glass, nylon, plastic or enameled glassware) with tightly closed or twisted lids, in a place protected from sunlight, at room temperature for no more than 5 days after preparation.

    1.5. The neutral anolyte complies with regulatory indicators of the safety and effectiveness of disinfectants, according to the requirements of SanPiN 21-112-9, does not have a toxic effect on the body and belongs to low-hazard chemical compounds (hazard class 4 according to GOST 12.1.007-76). It does not have an irritating effect on the skin, to a slight degree irritates the mucous membranes of the upper respiratory tract and eyes.

    1.6. Neutral anolyte has bactericidal, tuberculocidal, virucidal and fungicidal activity. It is effective against viruses and fungi at a concentration of 250 ± 50 mg / dm 3, tuberculosis mycobacteria - 350 ± 50 mg / dm 3, other bacteria - 250 ± 50 mg / dm 3 of active chlorine.

    1.7. Neutral anolyte is intended for disinfection of surfaces in rooms, dishes, underwear, overalls for personnel, toys, sanitary equipment, medical devices, cleaning equipment and materials for infections of bacterial, tuberculous, viral and fungal etiology. Disinfection modes are presented in table 1.

    2.2. Surfaces in rooms (floors, walls), surfaces of appliances, appliances, furniture, cleaning equipment, sanitary equipment (sinks, toilets, bathtubs, urinals, radiators, lighting fixtures, ventilation system grilles) are uniformly moistened with anolyte in a neutral way 2 times wiping with rags with an interval of 15 minutes The consumption of anolyte neutral is 100 cm 3 per 1 m 2 of surface. Surface areas, as an object of disinfection, are determined in accordance with Appendix 5 to the Order of the Ministry of Health of the Republic of Belarus No. 165 of November 25, 2002.

    2.3. Unassembled medical devices are completely immersed in a container with anolyte neutral. In the presence of cavities and channels, they are filled with a syringe, pipette or other devices, while removing air bubbles. The disinfectant solution layer above the product must be at least 1 cm.

    2.4. Dinnerware is freed from food debris and completely immersed in a container with anolyte neutral at a rate of 2 dm 3 per 1 set. Laboratory glassware is immersed in anolyte neutral. The disinfectant level must be at least 1 cm higher than the immersed dishes.

    2.5. Linen contaminated with biological fluids, staff overalls, dressings, and also cleaning materials are soaked in neutral anolyte containers at the rate of 4-5 dm 3 / kg of dry material.

    2.6. Toys, patient care items are completely immersed in neutral anolyte. The disinfectant layer must be at least 1 cm higher than the disinfected objects.

    2.7. After disinfection is complete, objects are washed. tap water.

    Table 1
    Disinfection modes of various objects with anolyte neutral (pH \u003d 6.2-7.2)
    Disinfection object
      Bacterial, viral and fungal etiology   Tuberculous etiology
    Concentration, mg / DM 3 Exposure, min Concentration, mg / DM 3 Exposure, min
      Medical devices from:
      -metal, glass;
      -plastics, rubber, etc.

    not< 200
      not< 200

    30
    60

    not< 300
    not< 300

    60
    90
    Tableware, laboratory not< 200 60 not< 300 90
    Surfaces (floors, walls, furniture, appliances, appliances, etc.) not< 200 60 not< 300 90
    Sanitary equipment (sinks, bathtubs, toilets, heating devices, lighting fixtures, etc.) not< 200 60 not< 300 90
    Overalls for staff (bathrobe, hat, shoe covers, etc.) not< 200 60 not< 300 90
    Underwear and bedding, diapers, dressings, etc. not< 200 60 not< 300 90
    Toys not< 200 60 not< 300 90
    Patient care items (oilcloths, enemas, vessels, etc.) not< 200 60 not< 300 90
    Cleaning equipment (mops, buckets, pans, etc.) not< 200 60 not< 300 90
    Cleaning materials (rags, napkins, etc.) not< 200 60 not< 300 90
    Rubber mats not< 200 60 not< 300 90

    3. Safety requirements when receiving anolyte neutral

    3.1. Operation of installations upon receipt of neutral anolyte should be carried out in a separate well-ventilated area. Collect anolyte in closed containers

    3.2. Personnel who have studied the Operation Manual of the Aquamed installation and have passed a medical examination in accordance with the Resolution of the Ministry of Health of the Republic of Belarus No. 33 of 08.08.2000 must be allowed to service the installation.

    When working with neutral anolyte, it is necessary to protect the skin of the hands with rubber gloves. For the duration of the exposure, the containers in which the immersion treatment is carried out are tightly closed with lids.

    3.3. When operating the installation, it is necessary to comply with the requirements set forth in GOST 12.2.025. Attendants should monitor the tightness of the connections and the condition of the equipment, cleanliness and order in the room. When working with anolyte neutral, you must follow the rules of personal hygiene. It is forbidden to smoke, drink and eat food in the workplace. After work, wash your face and hands with soap.

    3.4. Neutral anolyte must be stored separately from medicines.

    4.1. In case of violations of labor protection rules when working with anolyte neutral, personnel may develop acute poisoning, the signs of which are: redness and itching of the skin; headache.

    4.2. If there are signs of acute poisoning, it is necessary to: if possible, inhale in pairs a 2% solution of drinking soda (1 teaspoon per glass of water); see a doctor.

    4.3. If neutral anolyte gets into the eyes, they should be washed with plenty of water and consult a doctor; on the skin of the hands, wash them with water and grease with a softening cream.

    5. The list of possible errors in obtaining and using anolyte neutral and ways to eliminate them

    5.3. In violation of the disinfection regime (reduced chlorine concentration or exposure), the biocidal activity of the neutral anolyte decreases.

    Annex 1

    to “INSTRUCTIONS on the use of a neutral anolyte disinfectant solution, obtained at the AQUAMED-type plants manufactured by ChNPUP“ Akvapribor ”(Gomel, Republic of Belarus) in medical and preventive organizations.

    Anolyte quality control methods

    1. Sampling

    When sampling for quality control, the following conditions must be observed:

    the sample volume of the anolyte to determine the content of active chlorine should not be less than 500 cm 3 (in accordance with GOST 18190-77);

    the sample container must be airtight, made of inert material and completely filled.

    2. Determination of active chlorine

    2.1. Determination of active chlorine content by iodometric titration method in accordance with GOST 18190-72 “Drinking water. Methods for determination of residual active chlorine. "

    2.1.1. Equipment, materials and reagents:

    Laboratory glassware according to GOST 1770-74 and GOST 20292-74 with a capacity: volumetric flasks 100 and 1000 cm 3; pipettes without division 5, 10, 25 cm 3; microburette 5 cm 3; conical flasks with ground stoppers with a capacity of 250 cm 3 in accordance with GOST 25336-82;

    Distilled water according to GOST 6709-72;

    Sulfuric acid according to GOST 4204-77;

    Potassium dichromate according to GOST 4220-75;

    Soluble starch according to GOST 10163-76;

    Sodium thiosulfate.

    All reagents used in the analysis must be of pure qualification for analysis (analytical grade).

    2.1.2. Preparation for analysis:

    a) preparation of a 0.1 M sodium thiosulfate solution: 25 g of sodium thiosulfate are dissolved in freshly boiled and cooled distilled water and the volume is adjusted to 1 dm 3 in a volumetric flask;

    b) preparation of a 0 1 mol / dm 3 potassium dichromate solution: 4.904 g of potassium dichromate, weighed to an accuracy of +0,0002 g, recrystallized and dried at 180 ° C to constant weight, dissolved in distilled water and adjusted to 1 dm 3;

    c) preparation of 1 mol / dm 3 of sulfuric acid solution: carefully 28 cm 3 of concentrated sulfuric acid, add to 750 cm 3 of distilled water in small portions, cool and adjust the volume to 1 d 3;

    g) preparation of a 0.5% starch solution: 0.5 g of starch is mixed with a small volume of distilled water, poured into 100 cm 3 of boiling distilled water and boiled for several minutes;

    d) preparation of a 10% solution of potassium iodide: 10 g of potassium iodide are dissolved in distilled water and the volume is adjusted to 100 cm;

    f) determination of the correction coefficient of the sodium thiosulfate solution: 10 cm 3 of a 10% potassium iodide solution are placed in a 250 cm 3 conical flask, 20 cm 3 1 mol / dm 3 sulfuric acid solution and 10 cm 3 0.1 mol / dm 3 potassium dichromate solution are added . Stir and place the flask in a dark place for 5 minutes. The liberated iodine is titrated with 0.1 mol / dm 3 sodium thiosulfate solution in the presence of 1 cm 3 of starch until a turquoise color appears, which lasts at least 30 s. The correction factor (K) is calculated by the formula:

    and where a is the volume of sodium thiosulfate spent on titration, cm 3.

    2.1.3. Determination process: 5 cm 3 of 10% potassium iodide solution, 50 cm 3 1 mol / dm 3 sulfuric acid solution and 10 cm 3 anolyte are introduced into a conical flask with a ground stopper. The contents of the flask are mixed and placed in a dark place for 3-5 minutes. The liberated iodine is titrated with 0.1 mol / dm sodium thiosulfate solution until a light yellow color appears, after which 1 cm 3 of a 0.5% starch solution is added and titrated until the blue color disappears. The concentration of active chlorine (C ah, mg / DM 3) is calculated by the formula:

    C ah \u003d (V * K * 35.46 * 1000 * 0.1) / 10

    V is the volume of 0.1 mol / dm 3 of a sodium thiosulfate solution used for titration, cm 3; K is the correction factor for the molar concentration of the equivalent of a sodium thiosulfate solution; 10 - sample volume of anolyte taken for analysis, cm 3; 0.1 - molarity of sodium thiosulfate solution; 35.46 - the content of active chlorine corresponding to 1 cm 3 1 mol / DM 3 sodium thiosulfate solution.

    2.2. Determination of active chlorine by the express method using indicator paper.

    2 2.1. Equipment, materials and reagents:

    Indicator paper "Millichlor";

    Color scale.

    2.2.2. Definition: dip a strip of test paper into the test solution, put it on a white waterproof surface, and after 30-40 s compare the color of the strip with a color scale.

    2.3. Determination of active chlorine by the express method with potassium iodide.

    2.3.1. Equipment, materials and reagents:

    Crystals of potassium iodide (KI) according to GOST 4232-74, chemically pure;

    - "eye" spoon;

    Color scale.

    2.3.2. Definition: fill 1/2 of the tube with anolyte, add 1 "eye" spoon (5 mg) of potassium iodide, mix, compare with the color scale.

    3. Determination of pH

    3.1. Determination of the pH of the anolyte is carried out by the potentiometric method on the ionomer in accordance with the instructions attached to the device.

    3.2. Determination of pH by express method using universal indicator paper.

    3.2.1. Equipment, materials and reagents:

    Standard scale.

    3.2.2. Definition: immerse a strip of test paper in the test solution, then remove it and immediately compare the resulting color with a standard scale.

    INSTRUCTIONS on the use of neutral anolyte obtained on installations like "AQUAMED" for disinfection of swimming pools.

    Authors: I.I.Burak, A.B. Yurkevich, L.V. Polovinkin, Ananiev AC, Sedunov V.I., Vorokhobko CA, N.I. Miklis, N.V. Tkacheva, O.A. Kozyrevich, N.A. Tatarenko.

    The INSTRUCTION is intended for medical and technical personnel of the swimming pool, hygiene and epidemiology centers, disinfection centers and other institutions involved in disinfection activities.

    1. General information

    1.1. Neutral anolyte is a transparent liquid with a faint smell of chlorine, the main active components of which are highly active oxygen compounds of chlorine (ClO 2, HclO, NaClO, HClO 2, NaClO 2, etc.).

    1.2. Anolyte neutral complies with regulatory indicators of safety and effectiveness of disinfectants for disinfecting swimming pool water, according to the requirements of SanPiN 21-112-99 (p. 1.3, 2.3), does not have a toxic effect on the body and belongs to low-hazard chemical compounds (hazard class 4 according to GOST 12.1.007-76). It does not have an irritating effect on the skin, to a slight degree irritates the mucous membranes, membranes of the upper respiratory tract and eyes.

    1.3. Anolyte neutral has bactericidal, tuberculocidal, virucidal and fungicidal activity.

    1.4. These instructions regulate the use of neutral anolyte, obtained at Aquamed installations, as a disinfectant for disinfecting swimming pool water, preventive disinfection of rooms and equipment, disinfection of a pool bath after draining and mechanical cleaning. Neutral anolyte is a chlorine-containing substance, characterized by physicochemical properties that allow it to be used as a substitute for chlorine-containing preparations used to disinfect pool water.

    1.5. The instructions regulate the quality control of anolyte neutral in the content of active chlorine, the use of anolyte for disinfection of water, premises and equipment of the pool and the monitoring of the effectiveness of disinfection.

    1.6. The main documents regulating personal hygiene measures, sanitary-hygienic, anti-epidemic and sanitary-technical measures during the operation of swimming, swimming and sports swimming pools are SanPiN "Hygienic requirements for the design, operation and quality of swimming pools" No. 2.1.2.10-39- 2002.

    1.7. Water disinfection, preventive disinfection of rooms and equipment, pool bath disinfection is carried out by specially trained pool personnel or local disinfectants on a contractual basis with systematic laboratory monitoring at the production laboratory with regular at least 1 time per month and according to epidemiological indications by the state sanitary inspection.

    1.8. Responsibility for compliance with the sanitary-hygienic regime of operation of swimming pools and the use of neutral anolyte as a disinfectant lies with the administration of the pool.

    2. Preparation of a neutral anolyte disinfectant solution.

    2.1. A neutral anolyte disinfectant solution is obtained by electrochemical activation in Aquamed units (TU RB 490085159.002-2003) from aqueous solutions of chlorides (NaCl, KC1, etc.) in accordance with the Passport AGPTZ.293.000 PS. The installation allows you to get a neutral anolyte with an active chlorine content of 200 - 2000 mg / DM 3 and pH \u003d 6.2 - 7.2.

    2.2. The prepared solution of neutral anolyte is pre-stored and stored in a separate sealed container of chlorine-resistant material (plexiglass, polyethylene, vinyl plastic, polyvinyl chloride, etc.) at room temperature for no more than 5 days after preparation.

    2.3. The quality control of anolyte neutral is carried out upon commissioning of the installation and subsequently monthly in the chemical laboratory, and self-monitoring is carried out daily and when the operating mode is changed by the express method in accordance with clauses 3.3 and 3.4.

    2.4. Precautions when working with anolyte neutral are described in the passport for the installation "Aquamed".

    3.1. Sampling is carried out in a sealed container of inert material, which is completely filled, the anolyte sample volume for determining the active chlorine content must be at least 500 cm 3 (in accordance with GOST 18190-77);

    3.2. Determination of active chlorine.

    Color scale.

    3.3.2. Definition progress:

    Measured glass laboratory glassware in accordance with GOST 1770-74 and GOST 20292-74 with a capacity of: test tubes 15 cm 3.

    Crystals of potassium iodide (Kl) according to GOST 4232-74, chemically pure;

    - "eye" spoon;

    Color scale.

    4. Chlorination of the pool with anolyte neutral.

    4.1. Chlorination of pool water with anolyte, like any other chlorine-containing preparation, should be based on a preliminary determination of the chlorine absorption of water, calculation of the working dose of anolyte introduced into the pool water, and determination of the concentration of residual chlorine in the water. A constant concentration of residual chlorine in the sports pool should be maintained at the level of 0.3 - 0.5 mg / l, in the rest - 0.5 - 0.7 mg / l.

    In the pool bath for children 1-6 years old, the content of free residual chlorine is allowed at the level of 0.1 - 0.3 mg / l in the absence of coliphages in water.

    4.2. Over a long period (more than 2 hours), an increased content of residual free chlorine is allowed up to 1.5 mg / l, bound up to 2 mg / l. By the beginning of the reception of visitors, the concentration of residual chlorine should not exceed the standard level.

    4.3. During daily cleaning, the equipment and surfaces of the toilet, shower rooms, dressing rooms, walkways, benches, door handles, handrails, rugs, etc. are disinfected with neutral anolyte with a residual chlorine concentration of 200 mg / l by two times rubbing with a rag with a disinfectant flow rate of 200 ml per 1 sq. m at the surface.

    General cleaning of all rooms with subsequent disinfection is carried out at least 1 time per month.

    Disinfection of the bath after draining the water and mechanical cleaning is carried out by neutral anolyte with an active chlorine concentration of 200 mg / l, double irrigation with a disinfectant flow rate of 200 ml per 1 sq. m surface. The disinfectant is washed off with hot water no earlier than 1 hour after its application.

    4.4. During operation of the pool, neutral anolyte is added to the circulation system continuously or periodically using an ejector connected to the storage tank.

    4.5. Determination of chlorine absorption by water of anolyte neutral chlorine. The equipment, materials and reagents are the same as those used to control the concentration of residual chlorine in the pool water (section 5.3).

    Three liter flasks are poured per liter of pool water and anolyte is added in volumes containing 1, 2, 3 mg of active chlorine, respectively, in the first, second and third samples. The contents of the flasks are thoroughly mixed, aged for 30 minutes and the amount of residual chlorine is determined by the iodometric method. Chlorine demand is calculated taking into account the chlorine absorption of water and the dose of residual chlorine. Recalculate the volume of the anolyte on the volume of the pool and enter its required amount using a dispenser.

    Example: suppose that the working dose of anolyte, taking into account the chlorine needs of water, was 2 mg / l of active chlorine, or in terms of the volume of anolyte containing 200 mg / l of active chlorine, 10 ml of anolyte per 1 liter of water, or 10 l per 1 cubic meter. m of water. If the volume of the pool is 1000 cubic meters. m, you need anolyte 10 cubic meters. m

    5. Monitoring the effectiveness of disinfection of pool water with anolyte neutral

    5.1. The concentration of residual active chlorine is checked in the pool water every 2 hours.

    5.2. Water sampling is carried out in at least 2 points (in shallow and deep parts).

    5.3. Determination of residual chlorine is carried out according to GOST 18190-72 by the iodometric method.

    6. Signs of poisoning and first aid

    6.1. In case of violation of labor protection rules when working with anolyte neutral, personnel may develop acute poisoning, the signs of which are:

    respiratory irritation (sore nose and nasopharynx, acute persistent cough, nasal discharge);

    irritation of the mucous membranes of the eyes (burning, pain, itching, profuse lacrimation);

    redness and itching of the skin; I

    headache.

    6.2. When signs of acute poisoning appear:

    urgently take the victim to a well-ventilated area or to fresh air;

    provide him with peace and warming;

    give a warm drink (milk with mineral alkaline water or drinking soda);

    if possible, inhale in pairs a 2% solution of drinking soda (1 teaspoon per glass of water); consult a doctor.

    6.3. If neutral anolyte gets into the eyes, they should be washed with plenty of water and consult a doctor; on the skin of the hands - wash them with water and lubricate with a softening cream.

    7. The list of possible errors in the preparation and use of anolyte neutral

    7.1. With the wrong choice of the dose of sodium chloride, increased or reduced specific consumption of electricity, anolyte can be obtained with an insufficient concentration of active chlorine and other active substances, as well as with an acidic or alkaline reaction of the medium.

    7.2. In case of violation of the method of using anolyte neutral (uneven wetting of the surfaces, incomplete immersion or soaking), the biocidal activity of the disinfectant may decrease.

    7.3. In violation of the disinfection regime (reduced chlorine concentration or exposure), the biocidal activity of the neutral anolyte decreases.

    7.4. When using anolyte with an acid reaction, corrosion of metal products is possible. To reduce the corrosion ability when processing metal products, only neutral anolyte should be used, and if necessary, corrosion inhibitors (0.14% sodium oleate solution) should be used.

    INSTRUCTIONS on the use of neutral anolyte obtained on installations like "AQUAMED" for the disinfection of trade enterprises, public catering and market entities.

    INSTRUCTION developed by Vitebsk State Medical University, Republican Scientific and Practical Center for Hygiene, Vitebsk Regional Center for Hygiene, Epidemiology and Public Health, Private Scientific-Production Unitary Enterprise "AQUAPRIBOR", Gomel.

    Authors: I.I. Burak, A. B. Yurkevich, L. V. Poloviikin, Ananiev AC, T. N. Bondareva, P. V. Shelemei, N. Ya. Krasovsky, N. I. Miklis, N. A. . Tatarenko.

    The INSTRUCTION is intended for personnel of trade enterprises, public catering and market entities, as well as specialists of disinfection centers, hygiene and epidemiology centers and other institutions involved in disinfection activities.

    1. General information

    1.1. A neutral anolyte disinfectant solution is obtained by electrochemical activation in Aquamed installations (TU RB 490085159.002.2003) from aqueous solutions of chlorides (NaCl, KC1, etc.) in accordance with the Operation Manual. The installation allows you to get anolyte with an active chlorine content of 200 - 400 mg / DM 3 and pH \u003d 6.2-7.2.

    1.2. Neutral anolyte is a transparent liquid with a faint smell of chlorine, the main active components of which are highly active oxygen compounds of chlorine (ClO 2, HclO, NaClO, HClO 2, NaClO 2, etc.).

    1.3. The quality control of the neutral anolyte is carried out upon commissioning of the installation and subsequently monthly in the chemical laboratory, and self-monitoring - daily and when the operating mode is changed by the express method.

    1.4. Prepared solutions of neutral anolyte are stored in sealed containers of inert materials (glass, nylon, plastic or enameled glassware) with tightly closed or twisted lids, in a place protected from sunlight, at room temperature for no more than 5 days after preparation.

    1.5. Anolyte neutral complies with regulatory indicators of the safety and effectiveness of disinfectants, according to the requirements of SanPiN 21-112-9; does not have a toxic effect on the body and belongs to low-hazard chemical compounds (hazard class 4 according to GOST 12.1.007-76). It does not have an irritating effect on the skin, to a slight degree irritates the mucous membranes of the upper respiratory tract and eyes.

    1.6. Anolyte neutral has a bactericidal, including tuberculocidal, activity, virucidal and fungicidal activity.

    1.7. Anolyte neutral It is intended for disinfection of surfaces in rooms, dishes, industrial equipment, refrigeration equipment, technological equipment, sanitary equipment, industrial and cleaning equipment, materials, etc. for infections of bacterial, viral and fungal etiology. Disinfection modes are presented in table 1.

    Table 1
    Disinfection modes of various objects of trade enterprises, public catering and market entities anolyte neutral (pH \u003d 6.2-7.2)

    Disinfection object

    Infections disinfection modes:

    bacterial, viral and fungal etiology

    Concentration, mg / DM 3

    Exposure, min

    Inventory (trade, production) from:

    Metal, glass;

    Plastics, rubber, etc.

    Equipment (commercial, refrigerating, technological) from:

    Metal, glass;

    Plastics, rubber, etc.

    Trays, sinks, racks, trade counters from:

    Metal, glass;

    Plastics, rubber, etc.

    Scales, juice and drink dispensers, milk, coffee, cocoa vending machines

    Surfaces (floor, walls)

    Sanitary equipment (sinks, tanks, toilets, heaters, lighting fixtures, etc.)

    Cutting boards, decks

    Cleaning materials (mops, buckets, basins, pots, rags, napkins, etc.)

    2. The use of anolyte neutral

    2.1. Anolyte neutral should be used once without dilution.

    2.2. Surfaces in rooms (floors, walls), surfaces of production and refrigeration equipment, furniture, sanitary equipment (sinks, toilets, bathtubs, urinals, heating devices, lighting fixtures, ventilation system grilles) are uniformly moistened with anolyte in a neutral way by 2 times wiping with rags with an interval of 15 minutes Anolyte consumption is 100 cm3 per 1 m 2 of surface.

    2.3. The disassembled production equipment and inventory are completely immersed in a container with anolyte neutral. In the presence of cavities and channels, they are filled with a syringe, pipette or other devices, while removing air bubbles. The layer of disinfectant solution above the product must be at least 1 cm.

    2.4. The dishes are completely immersed in a container with anolyte neutral. The disinfectant level above the dishes must be at least 1 cm.

    2.5. Harvesting materials are completely immersed in neutral anolyte at the rate of 4 dm3 / kg of dry material.

    2.6. After disinfection is completed, the objects are washed with tap water for 1-3 minutes.

    2.4 Precautions when working with neutral anolyte are described in the passport for the installation "Aquamed".

    3. Quality control methods of anolyte neutral.

    3.1. Sampling is carried out in a sealed container of inert material, which is completely filled, the anolyte sample volume for determining the active chlorine content must be at least 500 cm3 (in accordance with GOST 18190-77);

    3.2 Determination of active chlorine

    3.2.1. Determination of active chlorine content by iodometric titration method in accordance with GOST 18190-72 “Drinking water. Methods for determination of residual active chlorine. "

    3.3. Determination of active chlorine by the express method using indicator paper.

    3.3.1. Equipment, materials and reagents:

    Indicator strips DESICONT-NA-01-P-150 NPF Vinar;

    Color scale.

    3.3.2. Definition progress:

    dip the indicator strip in the test solution, put it on a white waterproof surface and after 60 s compare the color of the strip with a color scale.

    3.4. Determination of active chlorine by the express method with potassium iodide. 3.4.1. Equipment, materials and reagents:

    Measured glass laboratory glassware in accordance with GOST 1770-74 and GOST 20292-74 with a capacity of: test tubes 15 cm 3.

    Crystals of potassium iodide (Kl) according to GOST 4232-74, chemically pure;

    - "eye" spoon;

    Color scale.

    3.4.2. Progress of determination: fill 1/2 of the tube with anolyte, add 1 "eye" spoon (5 mg) of potassium iodide, mix, compare with the color scale.

    3.5. PH determination

    3.5.1. Determination of the pH of the anolyte is carried out by the potentiometric method on the ionomer in accordance with the instructions attached to the device.

    3.6. Determination of pH by express method using universal indicator paper.

    3.6.1. Equipment, materials and reagents:

    Universal indicator paper;

    Standard scale.

    3.6.2. Definition: immerse a strip of test paper in the test solution, then remove it and immediately compare the color obtained with the standard scale.

    4. Signs of poisoning and first aid

    4.1. In case of violation of labor protection rules when working with anolyte neutral atpersonnel may develop acute poisoning, the signs of which are:

    respiratory irritation (sore nose and nasopharynx, acute persistent cough, nasal discharge);

    irritation of the mucous membranes of the eyes (burning, pain, itching, profuse lacrimation);

    redness and itching of the skin;

    headache.

    4.2. When signs of acute poisoning appear:

    urgently take the victim to a well-ventilated area or to fresh air;

    provide him with peace and warming;

    give a warm drink (milk with mineral alkaline water or drinking soda);

    if possible, inhale in pairs a 2% solution of baking soda, a teaspoon in a glass of water);

    see a doctor.

    4.3. If neutral anolyte gets into the eyes, they should be washed with plenty of water and consult a doctor; on the skin of the hands - wash them with water and lubricate with a softening cream.

    5. The list of possible errors in the preparation and use of anolyte neutral

    5.1. With the wrong choice of the dose of sodium chloride, increased or reduced specific consumption of electricity, anolyte can be obtained with an insufficient concentration of active chlorine and other active substances, as well as with an acidic or alkaline reaction of the medium.

    5.2. In case of violation of the method of using anolyte neutral (uneven wetting of the surfaces, incomplete immersion or soaking), the biocidal activity of the disinfectant may decrease.

    5.3. If the disinfection regimen is violated (reduced chlorine concentration or exposure), the biocodal activity of the neutral anolyte decreases.

    5.4. When using anolyte with an acid reaction, corrosion of metal products is possible. To reduce the corrosion ability when processing metal products, only neutral anolyte should be used, and if necessary, corrosion inhibitors (0.14% sodium oleate solution) should be used.

    I affirm: Head of department
       State Sanitary and Epidemiological Supervision Ministry of Health of Russia
       A.A. Monisov
       02/14/1997
       N MU-17-12
       MINISTRY OF HEALTH OF THE RUSSIAN FEDERATION

      1. GENERAL PROVISIONS.

    1. ANK neutral anolyte (hereinafter referred to as anolyte) produced in the STEL-10N-120-01 installation (hereinafter referred to as the installation) by electrochemical treatment of a sodium chloride solution in drinking water, is a colorless transparent liquid with the smell of chlorine, containing highly active oxygen compounds of chlorine, etc.
         Depending on the purpose, anolyte is prepared and used with an active chlorine content of 0.01%, 0.02%, 0.05% and a pH value of 7.2 to 8.4.
         Monitoring of these parameters should be carried out during commissioning of the installation, as well as during its operation after each switching to a different operating mode (saline flow rate, current strength) to obtain anolyte with another specified (from the above) concentration of active chlorine, but not less once a month. The anolyte quality control methodology is given in Appendix 2.
      Anolyte is used without dilution, once.
         The anolyte has a shelf life of 5 days if stored in a closed glass, plastic or enamelled container (without damaging the enamel) at room temperature in places protected from direct sunlight.
    2. Anolyte has antimicrobial (bactericidal, tuberculocidal, virucidal, fungicidal, sporocidal) and detergent properties.
    3. Anolyte is used to disinfect various objects (indoor surfaces, patient care items, dishes, linen, toys, sanitary equipment, cleaning material) for bacterial infections (including tuberculosis), viral (including hepatitis with a parenteral transmission mechanism, HIV infection ) and fungal (including candidiasis, dermatophytosis) etiology, as well as for disinfection, pre-sterilization cleaning and sterilization of medical devices made of glass, plastic, rubber, metals (titanium alloys).
         The process of disinfection of medical devices can be combined with the process of their pre-sterilization cleaning.

    2. APPLICATION OF ANOLYTE FOR DISINFECTION

    1. Anolyte disinfection is carried out by wiping (surfaces on the premises, sanitary equipment) and immersion (medical devices, patient care items, dishes, underwear, toys, cleaning material).
    2. Anolyte disinfection regimens for infectious diseases of various etiologies are presented in Table 1.
    3. The surfaces in the premises (floor, walls, hard furniture), sanitary equipment are wiped once or twice (with an interval of 15 minutes) with a rag abundantly dampened with anolyte. The surfaces to be treated should be evenly moistened. The rate of anolyte consumption for a single rubbing is 200 ml, for a double rubbing (total amount) - 300-400 ml per 1 m 2 of the treated surface. Heavily contaminated sanitary equipment is pre-cleaned with a ruff moistened with anolyte.
    4. Medical products are completely immersed in the anolyte, filled with the help of auxiliary means (syringe, pipette) cavities and channels of the products, while removing air bubbles. Detachable products are disinfected disassembled. After the end of disinfection exposure, the products are washed for 1 minute flowing drinking water  or incubated in a container of water for 1 minute with the filling of cavities and channels of products with water.
    5. Patient care items are completely immersed in anolyte. After disinfection is completed, they are washed with running water until the smell of chlorine disappears.
    6. Dishes are freed from food debris and completely immersed in anolyte. The anolyte consumption rate is 2 liters per 1 set (two plates, a cup or a glass). After disinfection, the dishes are washed with running drinking water for 1 minute per each item or kept in a container of water for 1 minute when completely immersed. Dishes made of metal are not subject to disinfection with anolyte.
    7. Linen is completely immersed in anolyte. The consumption rate of 5 liters per 1 kg of dry linen. After disinfection, the laundry is washed and rinsed in water.
    8. The toys are completely immersed in the anolyte and, after the end of the disinfection exposure, washed with running water until the smell of chlorine disappears.
    9. Harvesting material (rags) is completely immersed in the anolyte. After the end of disinfection exposure, the cleaning material is rinsed in water and dried.
    10. The disinfection quality control methodology is described in Appendix 3.

    Table 1. Modes of disinfection of various objects with anolyte

    Disinfection object Disinfection mode when The method of disinfection
       bacterial infections (excluding tuberculosis) and viral etiology tuberculosis fungal infections
    active concentration
      chlorine%
    disinfection time, min active concentration
      chlorine%
    disinfection time, min active concentration
      chlorine%
    disinfection time, min
    Indoor surfaces (floor, walls, hard furniture 0,02 120* 0,02
    0,05
    360
    90
    0,02
    0,05
    120
    30
    Wiping
    Medical devices ** from:
    - glass, metals 0,02 180 0,05 30 0,05 30 Immersion
    - plastics, silicone rubber 0,02 60 0,02
    0,05
    180
    30
    0,02
    0,05
    240
    30
    Immersion
    - rubber based on natural rubber 0,05 60 0,02
    0,05
    240
    120
    0,02
    0,05
    240
    60
    Immersion
    Patient Care Items *** 0,02
    0,05
    180***
    60
    0,02
    0,05
    0,05
    180***
    30***
    120
    0,02
    0,05
    0,05
    240
    30***
    60
    Immersion
    Tableware
      - no food residue 0,02 60 Immersion
    - with leftover food 0,02 360 0,02
    0,05
    360
    60
    0,02
    0,05
    360
    60
    Lingerie:
    - unpolluted 0,02 60 0,02 240 Immersion
    - polluted 0,02 360 0,05 180 0,05 60
    Toys *** 0,02
    0,05
    180***
    60
    0,05 60 0,05 60 Immersion
    Sanitary equipment 0,05 60* 0,05 120 0,02
    0,05
    240
    30
    Wiping
    Harvesting material (rags) 0,02 360 0,05 180 0,05 60 Immersion

    * - Disinfection is carried out by the method of double wiping with an interval of 15 minutes The total disinfection time is indicated taking into account the 15 - minute interval between wipes.
       ** - To combine the process of disinfecting medical devices with the process of their pre-sterilization cleaning with anolyte (clause 1.4.) After the end of the exposure time of the anolyte specified in this table for the corresponding infectious disease, it is necessary to perform the steps of pre-sterilization cleaning (clause 4.2., Table. 2) following the stage of soaking in anolyte.
      *** - In addition to products made from rubber based on natural rubber.

    3. APPLICATION OF ANOLITH FOR PRE-STERILIZATION CLEANING OF MEDICAL APPLICATIONS

    1. For pre-sterilization cleaning of medical devices, anolyte with an active chlorine concentration of 0.01% and 0.02% is used.
    2. Pre-sterilization cleaning is carried out manually in accordance with the following steps:
         - soaking in the anolyte when the products are completely immersed in the anolyte and thoroughly filling the channels and cavities with the help of various auxiliary means (syringe, pipette, etc.);
         - washing of each product in the anolyte used for soaking: the outer and accessible inner surfaces - with a cotton-gauze swab, cloth or ruff, channels - with a syringe;
         - rinsing products with washing channels with running drinking water;
         - rinsing products with washing channels with distilled water.
    3. Modes of pre-sterilization cleaning of medical devices are given in table. 2, quality control - see Appendix 4.

    Table 2. Modes of pre-sterilization cleaning of medical devices

    Processing object
    Products from:
    The concentration of active chlorine,% Duration of the stage, min.
      soaking
    anolyte
    washing of each product in anolyte rinsing with running drinking water rinsing distillation
    water
      - glass 0,01 30 0,5 1,0 0,5
    0,02 20 0,5 1,0 0,5
      - plastics 0,02 20 0,5 1,0 0,5
      - metals (simplest instruments from titanium alloys) 0,01 30 0,5 1,0 0,5
    0,02 20 0,5 1,0 0,5
      - rubber based on silicone rubber 0,01 30 0,5 1,0 0,5
    0,02 20 0,5 1,0 0,5
      - rubber based on natural rubber 0,01 30 0,5 1,0 0,5
    0,02 20 0,5 1,0 0,5

    4. APPLICATION OF ANOLYTE FOR STERILIZATION OF MEDICAL PURPOSE PRODUCTS

    1. Sterilization of medical devices with anolyte is carried out in enameled (without damage to the enamel), glass or plastic containers, which are closed with lids, when the products are completely immersed in the anolyte, ensuring that they thoroughly fill all channels and cavities of the products. To better fill the channels with anolyte and to more completely remove air bubbles from them, use syringes, pipettes or other auxiliary means. Detachable products are immersed in the anolyte disassembled. Sterilized products should be freely placed in containers with anolyte; the thickness of the anolyte layer above the products should be at least 1 cm.
    2. The sterilization modes of medical devices are given in table 3.
    3. During sterilization (including the stage of washing products from product residues), all manipulations are performed in compliance with aseptic conditions.
    4. After the end of the sterilization exposure time, the products are removed with sterile forceps (forceps) from the anolyte, removing it from the channels and cavities, and transferred to a sterile container with sterile drinking water to wash the products from product residues. Washing is carried out for 1 min with complete immersion of the products in water with the filling of channels and cavities with water.
    5. The sterile products washed from the anolyte residues are removed from the water, placed in a sterile sheet, the remaining water in the channels is removed using a sterile syringe or other device, and the products are transferred to a sterile sterilization box lined with a sterile sheet. The shelf life of sterilized products is not more than three days.
    6. The containers and water used when washing sterile products from product residues are pre-sterilized by steam at a temperature of 132 ° C for 20 minutes.

    Table 3. Modes of sterilization of medical devices

    Annex 1. ANOLYT QUALITY CONTROL METHODS

    1. The quality of the anolyte is controlled by the concentration of active chlorine in the anolyte and the pH value.
    2. Determination of the concentration of active chlorine in the anolyte.
      1. Reagents used.
           - Potassium iodide according to GOST 4232 h.h., 10% aqueous solution.
           - Sodium sulfate (sodium thiosulfate) 5-water according to TU6 - 09-2540, 0.1 N. solution.
           - Sulfuric acid according to GOST 4204, 1 N. solution.
           - Soluble starch according to GOST 10163, 0.5% solution, prepared according to GOST4919.1.
           - Distilled water according to GOST 6709.
      2. Preparation for analysis.
           - Preparation of a 10% potassium iodide solution. 10 g of potassium iodide are dissolved in 90 ml of freshly prepared and cooled distilled water.
           - Cooking 1 n. sulfuric acid solution. 27 ml of concentrated sulfuric acid, carefully, in small portions, constantly stirring, added to 750 ml of distilled water, cooled and the volume in the volumetric flask was adjusted to 1 liter.
      3. Analysis.  In a conical flask with a ground stopper with a capacity of 250 ml make 10 ml of anolyte, 5 ml of a 10% solution of potassium iodide and 50 ml of 1 N. sulfuric acid solution. The contents of the flask are mixed and placed in a dark place for 5 minutes. The released iodine is titrated with 0.1 n. a solution of sodium sulfate until light yellow in color, after which 1 ml of a 0.5% starch solution is added and the solution is titrated until the blue color disappears.
      4. Processing the results.  Mass fraction of active chlorine X in percent is calculated by the formula
           X \u003d (Y-Y1) * 0.003546 * 100/10
           Where:
        Y - the volume is exactly 0.1 N. a solution of sodium sulfate, spent on titration of the analyzed anolyte, cm 3;
           U1 - the volume is exactly 0.1 n. sodium sulfate solution, used for titration of a control solution, cm 3;
           0,003546 - the mass of chlorine corresponding to 1 cm 3 exactly 0.1 N. sodium sulfate solution, g;
           10 - the mass of the analyzed samples of anolyte,
           The arithmetic mean of two parallel definitions is taken as the result of the analysis.
    3. Determination of the pH of the anolyte is carried out using the ionomer I-120.1 or "pH-150" in accordance with the instructions of the device.

    Appendix 2 DISINFECTION QUALITY CONTROL METHODOLOGY

    1. The quality of disinfection is evaluated after it is carried out by bacteriological examination of microbial contamination of treated objects in order to identify Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli bacteria.
    2. Sampling is carried out by the method of swabs.
      1. Surfaces (surface areas) of various objects (Section 2.2.) Are thoroughly wiped with sterile gauze wipes (wipe size 5x5 cm) moistened with a sterile neutralizer solution (0.5% sodium thiosulfate solution). After that, the napkin is placed in a sterile test tube with 10 cm 3 of the above sterile neutralizer solution and sterile glass beads, shaken for 5 minutes, avoiding wetting the cork.
      2. When controlling small objects (utensils, toys, etc.), washings are made from the surface of the entire object. With a large surface of objects (floors, walls, furniture, etc.), washings are made from an area of \u200b\u200bat least 100 cm 2.
      3. When controlling medical devices (except for products with channels and small products), washings are taken in a similar way according to the same methodology (Clause 2.1.) From the surface of the working part of the product. For products having functional channels, the working end is lowered into a sterile tube with a sterile neutralizer solution and the channel is washed 1-2 times with this solution using a sterile syringe or pipette. Small items during sampling are completely immersed in a test tube with a sterile neutralizer solution and shaken for 5 minutes. Control is subject to 1% of simultaneously processed products of the same name (but not less than three products).
    3. From flushing fluid (tubes with a solution of a neutralizer used in sampling), 0.1 ml inoculations are made on the surface of yolk-salt, blood agar, on Endo medium. Crops are kept in a thermostat at a temperature of 37 ° C. Results are taken into account after 48 hours.
    4. In the presence of colony growth on these media, the identified microorganisms are identified in accordance with the current methodological documents. In the absence of growth of microorganisms specified in paragraph 1, disinfection is considered effective.

    Appendix 3 QUALITY CONTROL OF PRE-STERILIZATION CLEANING OF MEDICAL PURPOSES

    1. The quality of the pre-sterilization cleaning of products is assessed by placing an amidopyrine or azopyram test for the presence of residual amounts of blood according to the procedures set forth in the Methodological Instructions for Pre-Sterilization Cleaning of Medical Products, respectively (approved by the USSR Ministry of Health 08.06.82, No. 28-6 / 13) and in the guidelines "Quality control of pre-sterilization cleaning of medical devices using azopyram reagent" (approved by the USSR Ministry of Health on 05.26.88, No. 28-6 / 13).
    2. Control is subject to 1% of simultaneously processed products of the same name (but not less than three products).
    3. If blood residues are detected (positive sample), the entire group of products from which the products were taken for control should be re-processed until a negative result is obtained.

    Description:  the solution developed in the STEL-10N-120-01 installation for disinfection, pre-sterilization cleaning and sterilization, ready for use.

    Production:  Russia

    Appointment:  Anolyte ANK is intended for the disinfection of various objects (indoor surfaces, patient care items, dishes, linen, toys, sanitary equipment, cleaning material) for bacterial infections (including tuberculosis), viral (including hepatitis with a parenteral transmission mechanism, HIV- infection, poliomyelitis, adenoviruses, SARS viruses, H5N1 bird flu, herpes) and fungal (including candidiasis, dermatophytosis) etiology, as well as for disinfection, pre-sterilization cleaning and sterilization of ed Medical products made of glass, plastic, rubber, metals (titanium alloys) in medical institutions. Anolyte Neutral ANK as a medicine is used as a solution for local and external use and treatment of wounds.

    Composition: contains highly active oxygen compounds of chlorine and other oxidants in the form of peroxide and hydroperoxide compounds, i.e. a mixture of highly active metastable (electrochemically activated) oxidants, quantified by the equivalent of “active chlorine”. Depending on the purpose, Anolyte ANK is prepared and used with a content of a mixture of oxidants in the equivalent of active chlorine of 0.01%, 0.02%, 0.03%, 0.05% and a pH value of 7.2 to 7.5.

    Consistency, properties:  ANK neutral anolyte produced in the STEL-10N-120-01 installation (TU 9451-689-05834388-2006) of various models by electrochemical treatment of a solution of sodium chloride in drinking water, is a colorless transparent liquid with a faint smell of chlorine.

    Packing:  glass and plastic containers with a volume of 0.4 to 20 liters.

    Microbiology:  Anolyte ANK has antimicrobial (virucidal, bactericidal, tuberculocidal, fungicidal, sporocidal) and detergent properties. In the presence of organic contaminants (feces, blood, etc.), the disinfectant activity of Anolyte ANK is reduced.

    Toxicity:  "Anolyte ANK" by the degree of exposure to the body belongs to the 4th class of low-hazard substances (according to GOST 12.1.007) when introduced into the stomach, applied to the skin, has little toxicity with parenteral administration. It does not have a local irritant effect on the skin and mucous membranes of the eyes (when washing).

    Application:  “Anolyte ANK” disinfection is carried out by means of wiping, soaking, immersion and irrigation. Use anolyte at room temperature. Wipe disinfection can be carried out in the presence of patients.

    Shelf life:  5 days if stored in a closed glass, plastic or enamelled (without damaging enamel) container at room temperature in places protected from direct sunlight.

    Storage conditions:  in a closed container, avoiding direct sunlight.

    We have a low price for Anolyte neutral ANC .. You can buy other disinfectants wholesale and retail using the basket on our website.

      Anolyte ANK has antimicrobial (virucidal, bactericidal, tuberculocidal, fungicidal, sporocidal) and detergent properties.

    Indications for use

       - treatment of skin, skin folds, mucous membranes with the aim of disinfecting and removing organic contaminants (sweat, sebaceous glands, other contaminants);

    Treatment of infected wounds, prevention of wound infection.

    Release form

    solution for local and external use; a bottle (bottle) for blood and blood substitutes 400 ml, a pack of cardboard 1.

    Pharmacodynamics

       Anolyte neutral ANC is an aqueous solution of a dilute solution of sodium chloride, passed through an electrochemical reactor that produces chlorine-oxygen and hydroperoxide oxidants (hypochlorous acid, hypochlorite ion, active oxygen compounds).

    Anolyte neutral ANK is non-toxic, has a high reaction and catalytic activity at a low concentration of active substances, disinfecting activity, detergent and anti-inflammatory properties.

    Anolyte neutral ANC accelerates the healing of infected purulent wounds.

    Pharmacokinetics

       Actively acting substances of the Anolyte neutral ANC with external, local application do not have a resorptive effect on the body.

    Contraindications

       - hypersensitivity to the components of the drug.

    Do not treat baselioma, skin cancer at the site of the intended treatment

    Side effects

       Allergic reactions.

    If the exposure time is longer than 15 minutes, skin irritation may occur.

    Dosage and administration

       Outwardly. Locally.

    The prepared solution is applied to a gauze cloth before intensive wetting and a cloth moistened with Anolyte neutral ANK is applied to the treated inflamed or healthy area of \u200b\u200bthe skin. The application time is 10 -15 minutes. The consumption of Anolyte neutral ANC during application therapy is 40-70 ml per 1000 cm2 of skin surface, which corresponds to a dose of active substances from 4 to 7 mg - when calculated on a person’s body weight about 0.06-0.1 mg / kg of body weight per application. After application, the skin area treated with Anolyte neutral ANC is dried for several minutes and treatment is continued with other methods at the choice of the attending physician (dry sterile dressing, fat dressings, ointment dressings or other methods). The total number of applications with anolyte 2-3 times a day. The duration of the treatment is 5-7 days.

    Interactions with other drugs

       Do not use with iodine-containing antiseptics.

    Special instructions for admission

       It is possible to synthesize the drug in electrochemical plants of the STEL type ex tempore in the conditions of the operating unit, dressing room, treatment room, at the patient's bedside. The preparation prepared ex tempore is placed in clean sterile containers and used according to indications.

    Storage conditions

    In the dark place at a temperature of 15-25 ° C.
      Shelf life - 5 days from the date of manufacture of the drug.

    ATX Classification

    D Dermatotropic drugs

    D08 Antiseptics and disinfectants

    D08A Antiseptics and disinfectants

    D08AX Other antiseptics and disinfectants